This study is open-label dose expansion study to investigate the safety and toxicity of intravesical treatment of high-grade NMIBC (HGTa or CIS, including CIS with concomitant Ta) after transurethral resection of bladder tumor (TURBT) and/or biopsy using TARA-002 in adults unable to obtain intravesical Bacillus Calmette-Guérin (BCG), adults who have received at least one dose of intravesical BCG or adults who have received at least one dose of intravesical chemotherapy. After completion of the dose escalation phase (Phase 1a) and after the RP2D has been established, the dose expansion phase (Phase 1b) will start enrollment of subjects with CIS NMIBC with active disease to further evaluate the safety and preliminary efficacy of TARA-002, at the established RP2D. CIS NMIBC with active disease is defined as disease present at the last cystoscopic evaluation prior to signing the ICF. Subjects enrolled in the dose expansion phase will not include subjects previously enrolled and treated in the dose escalation phase. All subjects will receive 6 weeks of treatment at the established RP2D.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Phase 1b, Dose Expansion Phase: All subjects will receive 6 weekly doses of TARA-002 at the recommended Phase 2 dose (R2PD)
USC Norris Cancer Center
Los Angeles, California, United States
Mayo Clinic
Jacksonville, Florida, United States
Tulane Medical Center (TMC) - Clinic/Outpatient Facility
New Orleans, Louisiana, United States
Chesapeake Urology Research Associates
Baltimore, Maryland, United States
Mayo Clinic
Rochester, Minnesota, United States
Premier Medical Group of the Hudson Valley
Poughkeepsie, New York, United States
University of Rochester, Department of Urology
Rochester, New York, United States
Carolina Urologic Research Center
Myrtle Beach, South Carolina, United States
Urology Associates PC
Nashville, Tennessee, United States
UT Health San Antonio
San Antonio, Texas, United States
Phase 1b, Dose Expansion Phase: Incidence of AEs in subjects with CIS NMIBC with active disease
AE = adverse event
Time frame: Day 1 to Day 78
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